Ichthyosis prematurity syndrome in two Omani siblings, caused by homozygous c.1A > G mutation in the FATP4 gene

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Bibliographic Details
Published inInternational journal of dermatology Vol. 60; no. 3; pp. 368 - 371
Main Authors Al Mandhari, Hilal, Al-Musalhi, Buthaina, Al Mahroqi, Nouh, Hilmarsen, Hilde T, Braathen, Geir J, Khnykin, Denis
Format Report
LanguageEnglish
Published 01.03.2021
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Bibliography:ObjectType-Case Study-2
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ISSN:1365-4632
DOI:10.1111/ijd.15367